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The curse of modern brain science is that its founding father, Santiago Ram贸n y Cajal, was an incurable artist.

The Spanish neuroscientist felt that to see an object properly鈥攕ay, a Purkinje neuron, with its branches as luxurious as a sea fan鈥檚鈥攈e needed to draw it. But while his freehand pencil-and-ink sketches have mesmerized students of the brain for decades, they were not exact depictions of the cells he had so painstakingly stained and fixed under his microscope. They were interpretations; they were arguments. Cajal drew not just to see but to explain.

Today, more than 80 years after Cajal鈥檚 death, neuroscientists have traded their pencils for electron microscopes and MRI machines. These new tools also produce mesmerizing, multi-colored, often computer-animated images鈥攑ictures that have fueled countless scientific papers and popular accounts of progress in brain science. But they represent a looming trap.

Cajal鈥檚 task was to work out the basic microanatomy of the nervous system. He was the first to show that the brain contains billions of discrete cells, rather than an undifferentiated web of neural tissue.

Today鈥檚 neuroscientists are ready to probe deeper kinds of questions. Ultimately, they鈥檇 like to explain how perception, thought, and memory work. They want to know how 鈥渢he flower garden of the gray matter鈥� becomes a habitat for 鈥渢he mysterious butterflies of the soul,鈥� as Cajal framed the question in his . Ultimately, though, those are questions about function and integration, not just structure, and the explanations will not be found in images alone.

To visit The Beautiful Brain鈥攁 traveling exhibition of 80 of Cajal鈥檚 original drawings that landed in the fall of 2018 at the in Cambridge, Massachusetts鈥攊s to understand immediately why neuroscience, from its earliest moments, fell under the spell of visualization. Cajal鈥檚 drawings are diminutive, often no more than a few inches on a side (the museum supplies visitors with magnifying glasses). But they are alive with texture, depth, and whimsy. The viewer relates to Cajal鈥檚 delicate renderings of pyramidal neurons, astrocytes, and blood cells as if they were characters in a graphic novel about cellular survival.

To find another investigator who combined Cajal鈥檚 technical ingenuity, deftness with a pen, acuteness of perception, and perseverance, you鈥檇 have to go back to Leonardo da Vinci, the first person to systematically document human anatomy. Therein lies the burden of Cajal鈥檚 legacy.

The seeming precision of Cajal鈥檚 drawings gives them immense narrative power. They were the key weapons he used to overthrow the old reticular theory, which depicted the brain as a single massive network, in favor of his neuron doctrine. This success brought him the 1906 Nobel Prize in physiology or medicine. (Ironically, Cajal shared the prize with the Italian pathologist Camillo Golgi, who had invented the staining methods Cajal used to isolate neurons but who remained a lifelong proponent of the reticular theory.)

With Cajal鈥檚 drawings as inspiration, generations of neuroscientists seeking to understand the brain have turned to new visualization tools, such as functional magnetic resonance imaging (fMRI), that seem equally precise.

But there are at least two persistent pitfalls to this approach, neither of which was yet apparent in Cajal鈥檚 day.

The first is that visualization is always an act of imagination. Cajal had to capture his tiny subjects by hand because late-19th-century microphotography was not up to the task. But he did not always work from life, the way a painter composing a portrait might.

鈥淥ften, he would spend a morning at the microscope without sketching at all, and draw from memory in the afternoon,鈥� Lyndel King and Eric Himmel write in the companion book to The Beautiful Brain. (King is the director of the Weisman Art Museum, in Minneapolis, which curated the exhibit.)

No matter how accurate Cajal鈥檚 recall may have been, we know today that our memories are reconstructed and altered each time we bring them to mind. And Cajal鈥檚 editing went much further than this.

For emphasis, he represented some cells鈥攕uch as astrocytes, the gaudy, star-shaped support cells for which he had an understandable fondness鈥攁s much larger in relation to other cells than they actually are. He combined views from different slices of brain tissue. He presented time-lapse 鈥渁nimations,鈥� such as one of a white blood cell squeezing through a gap in a capillary wall. Many of his drawings 鈥渨ere wholly original compositions, mental reconstructions of a complex reality 鈥� [that show] many of the same aesthetic decisions an idealized portrait does,鈥� King and Himmel observe.

It鈥檚 no insult to Cajal to point out that his drawings were, in part, fabrications. They were intended for reproduction in his scientific books and journal articles, and were meant to instruct and influence his readers, not just to document what he saw.

Indeed, real brain tissue is such a mushy tangle of neurons, glial cells, and nerve fibers that it鈥檚 nearly impossible to represent it intelligibly without the kinds of simplifications Cajal introduced.

(Leonardo, too, resorted to shortcuts, assumptions, and synthetic views in his anatomical drawings. Shown here at right, his famous 鈥淪tudies of the Fetus in the Womb,鈥� now in the Royal Collection of the United Kingdom, shows interlocking, finger-like cotyledons in the walls of the uterus. But cotyledons are not found in the human uterus. Leonardo could only have seen them while dissecting a cow鈥檚 uterus.)

So representations are always tailored to explain and persuade. But today, the volume of data that must be harvested, curated, and compressed to create a single electron micrograph or fMRI image is vastly greater鈥攁nd for neuroscientists, the opportunities for exaggeration and self-deception have also multiplied.

As fMRI approaches its 30th birthday, this has become a familiar line of criticism鈥攐ne that was ably summarized and updated by University of Pennsylvania neurologist Geoffrey Aguirre in the 2014 Hastings Center special report 鈥淚nterpreting Neuroimages.鈥� Aguirre points out that the data for each voxel (3-D pixel) in an fMRI image undergoes multiple processing steps, including image stabilization; statistical comparisons to distinguish real brain signals from random fluctuations; 鈥渃leaning鈥� to throw out data below a certain threshold; smoothing to correct for differences between test subjects; and, finally, color-coded display against 2-D or 3-D .

鈥淲hile these steps are well justified from a scientific standpoint, in aggregate they have come to constitute an aesthetic: there is a certain way that neuroimaging results are 鈥榚xpected鈥� to look,鈥� Aguirre writes. This makes fMRI a slippery affair. The worry, as cognitive neuroscientist Martha Farah comments in the same , is that 鈥渢he images are more researcher inventions than researcher observations.鈥�

The second problem that has beset neuroscience since Cajal鈥檚 day is that neuroimaging studies too often proceed as if characterizing a structure or localizing an effect were the same as explaining it.

Cajal was studying dead tissue fixed in histological slides. Even so, his sheer powers of observation helped him answer a pressing functional question: how does information flow through individual neurons? By examining cells from the retina and the olfactory bulb鈥攑laces where the brain interfaces directly with the outside world鈥擟ajal was able to intuit (correctly) that electrical impulses, also called 鈥渁ction potentials,鈥� must flow from a neuron鈥檚 dendrites to its central cell body to its axon.

Alas, it鈥檚 not as obvious how patterns of activity across thousands or millions of neurons correlate with mental states or processes.

Functional MRI measures blood oxygenation levels in specific areas of the brain over time. This is thought to be an indicator of glucose metabolism, or how hard neurons are working. Images from fMRI studies can pin down changes in blood oxygenation with fairly high resolution鈥攁 typical voxel represents a 3x3x3 mm³ cube of brain tissue鈥攚hich makes it possible to map cognitive processes to specific regions. Work by MIT neuroscientist Nancy Kanwisher, for example, has shown that much of the processing behind facial recognition occurs in a thimble-sized region now called the fusiform face area, in the fusiform gyrus of the inferior temporal cortex.

Unfortunately, many neuroscience studies stop at localization. This is unsatisfying, to say the least, since the ability to assign an operation to a specific part of the brain tells us almost nothing about how the operation actually works.

鈥淚f an area 鈥榣ights up鈥� while a person is doing a task or solving a problem or memorizing a list of words, it could mean any number of things,鈥� points out Carole Wade, co-author of a leading undergraduate psychology textbook. 鈥淭hat area may be the sole locus of the operation; or it may have been disinhibited by some other area that is of equal or greater importance even though less active; or it may be necessary for a particular mental operation but not sufficient unless other areas are also involved鈥�. that a brain area 鈥榣ights up鈥� when someone is doodling, that doesn鈥檛 mean the area is a doodling center!鈥�

The most we can really conclude from fMRI images is that there are consistent patterns of brain activation when subjects are doing things like looking at faces or listening to speech. By integrating many of these patterns, our brains somehow give rise to conscious awareness. But given the amount of apparent redundancy and parallelism in neural networks, it will take a long time to figure out how this all works.

Make no mistake: functional MRI will continue to be an important tool in that pursuit. There are ways to counter and minimize many of the biases that can affect neuroimaging, and neuroscientists are no more prone to confuse observation and invention than, say, astronomers or particle physicists. , it鈥檚 possible to 鈥渆ncourage the fair and realistic evaluation of functional neuroimaging as a scientific method and to foster an understanding of imaging鈥檚 limitations without 鈥榯hrowing the baby out with the bathwater.鈥欌��

But it鈥檚 a welcome development that many of the newest techniques for understanding the brain鈥檚 functions were not born as imaging tools. Take optogenetics. Using tricks from gene therapy, neuroscientists can introduce light-activated or light-emitting ion channel proteins into the cell walls of specific neurons in live animals such as mice. Some of these proteins work as actuators, causing neurons to fire electrically in response to millisecond-scale flashes of light. Others are sensors that fluoresce when individual neurons fire, providing a readout of neuron-level activity. Though largely untested in humans, the technique is already helping neuroscientists determine which neurons figure in motor control, pain, fear, and various behaviors in animals.